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A Roadmap of In Vitro Models in Osteoarthritis: A Focus on Their Biological Relevance in Regenerative Medicine

期刊

JOURNAL OF CLINICAL MEDICINE
卷 10, 期 9, 页码 -

出版社

MDPI
DOI: 10.3390/jcm10091920

关键词

osteoarthritis; in vitro inflammatory models; biomechanical models; microfluidics models; cartilage; synovium; 3D scaffolds; regenerative medicine

资金

  1. Italian Ministry of Health

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Osteoarthritis (OA) is a prevalent musculoskeletal disorder worldwide, with articular cartilage and synovial membrane being key biological targets. Understanding the accuracy of preclinical in vitro OA models could lead to innovative approaches in regenerative medicine, bridging the gap between animal and human studies.
Osteoarthritis (OA) is a multifaceted musculoskeletal disorder, with a high prevalence worldwide. Articular cartilage and synovial membrane are among the main biological targets in the OA microenvironment. Gaining more knowledge on the accuracy of preclinical in vitro OA models could open innovative avenues in regenerative medicine to bridge major gaps, especially in translation from animals to humans. Our methodological approach entailed searches on Scopus, the Web of Science Core Collection, and EMBASE databases to select the most relevant preclinical in vitro models for studying OA. Predicting the biological response of regenerative strategies requires developing relevant preclinical models able to mimic the OA milieu influencing tissue responses and organ complexity. In this light, standard 2D culture models lack critical properties beyond cell biology, while animal models suffer from several limitations due to species differences. In the literature, most of the in vitro models only recapitulate a tissue compartment, by providing fragmented results. Biotechnological advances may enable scientists to generate new in vitro models that combine easy manipulation and organ complexity. Here, we review the state-of-the-art of preclinical in vitro models in OA and outline how the different preclinical systems (inflammatory/biomechanical/microfluidic models) may be valid tools in regenerative medicine, describing their pros and cons. We then discuss the prospects of specific and combinatorial models to predict biological responses following regenerative approaches focusing on mesenchymal stromal cells (MSCs)-based therapies to reduce animal testing.

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